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Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders.

Thiadens, A.A.H.J. and Den Hollander, A.I. and Roosing, S. and Nabuurs, S.B. and Zekveld-Vroon, R.C. and Collin, R.W.J. and De Baere, E. and Koenekoop, R.K. and Van Schooneveld, M.J. and Strom, T.M. and Van Lith-Verhoeven, J.J.C. and Lotery, A.J. and Van Moll-Ramirez, N. and Leroy, B.P. and Van den Born, L.I. and Hoyng, C.B. and Cremers, F.P.M. and Klaver, C.C. (2009) Homozygosity mapping reveals PDE6C mutations in patients with early-onset cone photoreceptor disorders. American Journal of Human Genetics, 85, 240-247. ISSN 0002-9297.

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Item Type:Article
Institutes:Netherlands Institute for Neuroscience (NIN)
ID Code:6599
Deposited On:10 Sep 2009 02:00
Last Modified:03 Aug 2010 14:32

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